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7. Suggest how you would synthesize the compound X shown below. Make sure that compound X...
8. Suggest how you would synthesize the compound X shown below. Pay a close attention to...
8. Suggest how you would synthesize the compound X shown below. Pay a close attention to the stereochemis try in the product! CI *see hint on question 7 nucleophile electrophile A. В. Na O nuceophile nucleophile electiophile electrophile С. D. Na O Na nucleophile electrophile electophile nucleaphile Е. nudeophile electrophile
Problem #3 Show how you would synthesize the compound represented in the Fischer projection below starting...
Problem #3 Show how you would synthesize the compound represented in the Fischer projection below starting from acetylene. You may use any other reagent necessary. HC-OH HC-OH Extra Credit When treated with hydrogen and a platinum catalyst, an unknown compound X absorbs 5 equivalents of hydrogen to give 7-butylcyclohexane. Treatment of X with an excess of ozone, followed by dimethyl sulfide and water, gives the products shown below. Propose a structure for X.
Can you help me identify reagent (i), Compound 8 and Compound 12 in the reaction scheme?...
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
1. Consider the SN2 reaction shown below and answer the following questions.nobl 8 acetone no t...
1. Consider the SN2 reaction shown below and answer the following questions.nobl 8 acetone no t iNaSCH SCH, + NaBr worl s1918. A. Write the rate law for the reaction. ebiler vil ar to nollurunoonoo oli nison. B. Identify the nucleophile and the electrophile in the reaction. HOCH lo noiden nog orgnismanl.d C. State how each of the following factors would affect the rate of the reaction. CHOW CHOOH glasa a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration...
Carbon NMR Question: [7 pts] Compound X (3c NMR provided below, with DEPT study info), whose...
Carbon NMR Question: [7 pts] Compound X (3c NMR provided below, with DEPT study info), whose molecular formula is C9HIiNO, was formed by the reaction of on acid chloride with an amine-containing compound (IR shown below), C7H9N. write the reaction equation, after determining the structures of the amine, acid halide and product (Compound X). Show work. No credit for reaction only. 13C NMR of product: 180 0401600 PPM DEPT-90: 121.5, 129.2 ppm DEPT-135: positive: 21.3, 24,121.5, 129.2; negative: none
need help with the boxed bullet point. writing the chemical reaction scheme for the experiment. Synthesis of an A...
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
Complete questions 10-27 PART II: REACTIONS: Here is another different" question. Pretend you have been asked...
Complete questions 10-27
PART II: REACTIONS: Here is another different" question. Pretend you have been asked by me to put together a bunch of one-step reactions WITH starting materials (your choice), reagents and answers to help me with writing a final exam. For example: let's say I ask you to give an example of a free radical chlorination with a non-cyclic compound. Below would be your answer. As I am pretty sure you can figure out, there are millions of...
8. Suggest how you would synthesize the compound X shown below. Pay a close attention to the stereochemis try in the product! CI *see hint on question 7 nucleophile electrophile A. В. Na O nuceophile nucleophile electiophile electrophile С. D. Na O Na nucleophile electrophile electophile nucleaphile Е. nudeophile electrophile
Problem #3 Show how you would synthesize the compound represented in the Fischer projection below starting from acetylene. You may use any other reagent necessary. HC-OH HC-OH Extra Credit When treated with hydrogen and a platinum catalyst, an unknown compound X absorbs 5 equivalents of hydrogen to give 7-butylcyclohexane. Treatment of X with an excess of ozone, followed by dimethyl sulfide and water, gives the products shown below. Propose a structure for X.
Can you help me identify reagent (i), Compound 8 and
Compound 12 in the reaction scheme?
You have laboratory data on all the compounds in the
synthesis, however the amount of data available to you varies. Some
have the entirety of the spectral data, others have as little as
the elemental analysis. Use the laboratory data to help you
discover which reaction has been performed.
The lab data for Compound 8 and 12 is as
follows:
You can use any...
1. Consider the SN2 reaction shown below and answer the following questions.nobl 8 acetone no t iNaSCH SCH, + NaBr worl s1918. A. Write the rate law for the reaction. ebiler vil ar to nollurunoonoo oli nison. B. Identify the nucleophile and the electrophile in the reaction. HOCH lo noiden nog orgnismanl.d C. State how each of the following factors would affect the rate of the reaction. CHOW CHOOH glasa a. Increasing the concentration of 1-bromopropane. b. Decreasing the concentration...
Carbon NMR Question: [7 pts] Compound X (3c NMR provided below, with DEPT study info), whose molecular formula is C9HIiNO, was formed by the reaction of on acid chloride with an amine-containing compound (IR shown below), C7H9N. write the reaction equation, after determining the structures of the amine, acid halide and product (Compound X). Show work. No credit for reaction only. 13C NMR of product: 180 0401600 PPM DEPT-90: 121.5, 129.2 ppm DEPT-135: positive: 21.3, 24,121.5, 129.2; negative: none
need help with the boxed bullet point. writing the chemical
reaction scheme for the experiment.
Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part I Pre-lab Assignment for Synthesis of an Alkyl Halide: A Nucleophilic Substitution Reaction, Part 1 1. From The Organic Chem Lab Survival Manual ( edition) by Zubrick • Review pages 201-204: Standard Reflux. • Review pages 127-140: Extraction • Review pages 164-189: Distillation, Simple Distillation. The Distillation Example, and The Distillation Mistake. 2. Read this...
Complete questions 10-27
PART II: REACTIONS: Here is another different" question. Pretend you have been asked by me to put together a bunch of one-step reactions WITH starting materials (your choice), reagents and answers to help me with writing a final exam. For example: let's say I ask you to give an example of a free radical chlorination with a non-cyclic compound. Below would be your answer. As I am pretty sure you can figure out, there are millions of...
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